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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 709838Generated: October 31, 2026

Hydrochloric Acid → 2-(Tert-butyldimethylsilyloxymethyl)-4-bromothiazole

https://huagongshe.com/reaction/709838

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantImidazoleHCID 795—
Reactanttert-Butyldimethylsilyl chlorideHCID 28928—
Reactant(4-Bromo-1,3-thiazol-2-yl)methanolHCID 11041630—
SolventTetrahydrofuranHCID 8028—
Product2-(Tert-butyldimethylsilyloxymethyl)-4-bromothiazoleHCID 16736579—

Reaction Steps

To a solution of (4-bromothiazol-2-yl)methanol (1.30 g) and imidazole (600 mg) in THF (10 mL) was added dropwise tert-butyldimethylchlorosilane (1.60 mL), and the mixture was stirred at room temperature for 1 hr. 1N Hydrochloric acid was added, and the reaction mixture was extracted with ethyl acetate. The extract was washed with saturated brine, and dried over anhydrous sodium sulfate. The solvent was evaporated under reduced pressure, and the residue was purified by silica gel column chromatography (ethyl acetate/hexane) to give the title compound (1.90 g) as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09181186B2
Source datasetuspto-grants-2015_11
ORD IDord-618f66ba255e432c8d4df778c0ed3d33
Source noteuspto-grants-2015_11